HGVS | Genome Assembly |
---|---|
NC_000016.10:g.88719583C= , CM000678.2:g.88719583C= | GRCh38 |
NC_000016.9:g.88785991C= , CM000678.1:g.88785991C= | GRCh37 |
NC_000016.8:g.87313492C= | NCBI36 |
NG_042229.1:g.70638G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301015.14:c.6462G= MANE Select | ENSP00000301015.9:p.Glu2154= | |
ENST00000466823.3:c.488G= | ||
ENST00000301015.13:c.6462G= | ENSP00000301015.9:p.Glu2154= | |
ENST00000419505.5:c.228G= | ENSP00000406358.1:p.Glu76= | |
ENST00000466823.2:c.488G= | ||
ENST00000495568.7:n.703G= | ||
ENST00000497793.2:n.617G= | ||
NM_001142864.2:c.6462G= | NP_001136336.2:p.Glu2154= | |
NM_001142864.3:c.6462G= | NP_001136336.2:p.Glu2154= | |
NM_001142864.4:c.6462G= MANE Select | NP_001136336.2:p.Glu2154= |